Elevate quality standards as a Quality Assurance Manager in Regulatory Affairs for medical devices. Lead QA activities and drive compliance in a fast-paced setting. In this leadership role, you will oversee daily Quality Assurance and Regulatory Affairs operations, ensuring they align with ISO 13485 requirements. With 5-10+ years of experience, you will coach a team, build cross-functional relationships, and establish KPIs for continuous improvement in quality metrics. Key Responsibilities:

- Lead day-to-day QA and Regulatory Affairs activities
- Establish goals and track quality objectives
- Coach and develop QA/RA team members
- Ensure audit readiness across various functions
- Directly execute critical QA/RA work hands-on Requirements:
- 5–10+ years in Quality Assurance leadership
- Experience in ISO 13485 environments
- Proven experience with audit management and CAPA systems
- Strong communication skills with stakeholders
- Background in engineering or science preferred Drive the success of regulatory compliance and quality management in the medical device sector.

📌 Quality Assurance Manager in Medical Devices (Burnaby)
🏢 Jobtailor
📍 Burnaby